HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305823Generated: November 2, 2026
Dimethyl Sulfoxide → HCID 13483105, compound
https://huagongshe.com/reaction/2305823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 1-Nitropropane | HCID 7903 | — |
| Reactant | Methyl 2-cyano-3-methylcrotonate | HCID 248907 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | HCID 13483105 | HCID 13483105 | — |
Reaction Steps
The title compound was synthesized similarly to J. Org. Chem. 50 (1985), 2807-2809: 5.6 g (50mmol) of potassium tert-butoxide were initially charged in 15 ml of dimethyl sulfoxide, and 4.4 g (50 mmol) of nitropropane dissolved in 190 ml of dimethyl sulfoxide were slowly added dropwise. After addition of 5 g (36 mmol) of methyl 2-cyano-3-methylbut-2-enoate dissolved in 10 ml of dimethyl sulfoxide, the mixture was stirred at room temperature for 40 hours. The reaction was quenched by slow addition of water. The reaction mixture was extracted three times with methyl tert-butyl ether. The organic phases were dried with magnesium sulfate and freed from ether giving the crude product (9 g), which was employed for the next reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06441044B1 |
|---|
| Source dataset | uspto-grants-2002_08 |
|---|
| ORD ID | ord-d596ae9026f747309866659b016b572f |
|---|
| Source note | uspto-grants-2002_08 |
|---|